AccessGUDID - DEVICE: V. Mueller (10885403130632)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: SU21062
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: SU21062
Company Name: STERIS CORPORATION

Primary DI Number: 10885403130632
Issuing Agency: GS1
Commercial Distribution End Date: November 06, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 021599373 *Terms of Use

Device Description: V. Mueller FRANKLIN-SILVERMAN BIOPSY NDLE OUTER CANN LGTH 6 inches 15.2CM CANNULA HUB LGTH 7-1/2 inches 19CM SPLIT NDLE HUB 8-1/4 inches 21CM

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
37462	Body aspiration needle, reusable	A sharp bevel-edged, hollow tubular metal instrument designed to remove fluid from a body cavity or to obtain a biopsy specimen from a patient through aspiration; it is not dedicated to a particular part of the anatomy. The device is typically longer than a hypodermic needle and usually has a wider hub. It is not intended for administration of pharmaceuticals. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FCG	Biopsy needle

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 8dd1c69e-a047-4b0d-beae-1009497da434
Public Version Date: November 07, 2024
Public Version Number: 7
DI Record Publish Date: September 24, 2016